Deymier Séverine, Louvat Camille, Fiorini Francesca, Cimarelli Andrea
Centre International de Recherche en Infectiologie (CIRI), Université de Lyon, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, École Nationale Supérieur de Lyon, France.
UMR 5086 - CNRS / UCBL, IBCP, Lyon, France.
FEBS Open Bio. 2022 Jun;12(6):1096-1111. doi: 10.1002/2211-5463.13382. Epub 2022 Feb 27.
Interferon-stimulated gene 20 kDa protein (ISG20) is a relatively understudied antiviral protein capable of inhibiting a broad spectrum of viruses. ISG20 exhibits strong RNase properties, and it belongs to the large family of DEDD exonucleases, present in both prokaryotes and eukaryotes. ISG20 was initially characterized as having strong RNase activity in vitro, suggesting that its inhibitory effects are mediated via direct degradation of viral RNAs. This mechanism of action has since been further elucidated and additional antiviral activities of ISG20 highlighted, including direct degradation of deaminated viral DNA and translational inhibition of viral RNA and nonself RNAs. This review focuses on the current understanding of the main molecular mechanisms of viral inhibition by ISG20 and discusses the latest developments on the features that govern specificity or resistance to its action.
干扰素刺激基因20千道尔顿蛋白(ISG20)是一种研究相对较少的抗病毒蛋白,能够抑制多种病毒。ISG20具有很强的核糖核酸酶特性,属于广泛存在于原核生物和真核生物中的DEDD核酸外切酶大家族。ISG20最初的特征是在体外具有很强的核糖核酸酶活性,这表明其抑制作用是通过直接降解病毒RNA介导的。此后,这一作用机制得到了进一步阐明,ISG20的其他抗病毒活性也得到了突出,包括直接降解脱氨基的病毒DNA以及对病毒RNA和非自身RNA的翻译抑制。本综述重点关注目前对ISG20抑制病毒的主要分子机制的理解,并讨论了决定其作用特异性或抗性的特征的最新进展。